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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945393Generated: November 1, 2026

1,2-Dichloroethane → HCID 16124851, compound

https://huagongshe.com/reaction/1945393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant3-AminobenzamideHCID 1645—
Reactant(4-Nitrophenoxy)acetic acidHCID 15720—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 16124851HCID 1612485182.7%

Reaction Steps

To a solution of (4-nitrophenoxy)-acetic acid (100 mg, 0.5 mmol), 3-amino benzamide (103.5 mg, 0.76 mmol), HOBt (102.81 mg, 0.76 mmol) and DIPEA (98.34 mg, 0.76 mmol) in DMF (2 ml) was added EDC (145.86 mg, 0.76 mmol) at room temperature and the resulting mixture was stirred until reaction completion as indicated by TLC. Reaction mixture was poured onto ice cold water, diluted with a mixture of MeOH:MC (10%), separated organic layer and sequentially washed with aqueous sodium bicarbonate, brine and water, and dried over anhydrous MgSO4. The solvent was filtered and evaporated under reduced pressure to afford a crude solid, which was purified flash chromatography on silica gel (MeOH:MC=1:9-2:8) to afford of 3-[2-(4-tert-butyl-phenoxy)acetylamino]-benzamide as a colorless solid (135 mg, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394799B2
Source datasetuspto-grants-2013_03
ORD IDord-85b01301f4b34013b01e69391c318b14
Source noteuspto-grants-2013_03